From fluorescence polarization to Quenchbody: Recent progress in fluorescent reagentless biosensors based on antibody and other binding proteins

被引:40
作者
Ueda, Hiroshi [1 ]
Dong, Jinhua [1 ]
机构
[1] Tokyo Inst Technol, Chem Resources Lab, Midori Ku, Yokohama, Kanagawa 2268503, Japan
来源
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS | 2014年 / 1844卷 / 11期
关键词
Reagentless biosensor; In vitro translation; Position-specific labeling; DARPin; Fluorescence quenching; Q-body; NONNATURAL AMINO-ACIDS; KNOWLEDGE-BASED DESIGN; ANKYRIN REPEAT PROTEIN; OPEN SANDWICH FLUOROIMMUNOASSAY; ANTIGEN-DEPENDENT FLUORESCENCE; CROSS-CORRELATION SPECTROSCOPY; SURFACE-TETHERED COMPONENTS; ENERGY-TRANSFER; IN-VITRO; INTERCHAIN INTERACTION;
D O I
10.1016/j.bbapap.2014.06.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Recently, antibody-based fluorescent biosensors are receiving considerable attention as a suitable biomolecule for diagnostics, namely, homogeneous immunoassay and also as an imaging probe. To date, several strategies for "reagentless biosensors" based on antibodies and natural and engineered binding proteins have been described. In this review, several approaches are introduced including a recently described fluorescent antibody-based biosensor Quenchbody, which works on the principle of fluorescence quenching of attached dye and its antigen-dependent release. The merits and possible demerits of each approach are discussed. This article is part of a Special Issue entitled: Recent advances in molecular engineering of antibody. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:1951 / 1959
页数:9
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